Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Translational Psychiatry
Gialluisi, Alessandro A; Andlauer, Till F M TFM; Mirza-Schreiber, Nazanin N; Moll, Kristina K; Becker, Jessica J; Hoffmann, Per P; Ludwig, Kerstin U KU; Czamara, Darina D; St Pourcain, Beate B; Brandler, William W; Honbolygó, Ferenc F; Tóth, Dénes D; Csépe, Valéria V; Huguet, Guillaume G; Morris, Andrew P AP; Hulslander, Jacqueline J; Willcutt, Erik G EG; DeFries, John C JC; Olson, Richard K RK; Smith, Shelley D SD; Pennington, Bruce F BF; Vaessen, Anniek A; Maurer, Urs U; Lyytinen, Heikki H; Peyrard-Janvid, Myriam M; Leppänen, Paavo H T PHT; Brandeis, Daniel D; Bonte, Milene M; Stein, John F JF; Talcott, Joel B JB; Fauchereau, Fabien F; Wilcke, Arndt A; Francks, Clyde C; Bourgeron, Thomas T; Monaco, Anthony P AP; Ramus, Franck F; Landerl, Karin K; Kere, Juha J; Scerri, Thomas S TS; Paracchini, Silvia S; Fisher, Simon E SE; Schumacher, Johannes J; Nöthen, Markus M MM; Müller-Myhsok, Bertram B; Schulte-Körne, Gerd G
Genome-wide screening for DNA variants associated with reading and language traits.
Genes, Brain, And Behavior
Gialluisi, A A; Newbury, D F DF; Wilcutt, E G EG; Olson, R K RK; DeFries, J C JC; Brandler, W M WM; Pennington, B F BF; Smith, S D SD; Scerri, T S TS; Simpson, N H NH; , ; Luciano, M M; Evans, D M DM; Bates, T C TC; Stein, J F JF; Talcott, J B JB; Monaco, A P AP; Paracchini, S S; Francks, C C; Fisher, S E SE